Indapamide - 0228-2571-96 - (Indapamide)

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Drug Information of Indapamide

Product NDC: 0228-2571
Proprietary Name: Indapamide
Non Proprietary Name: Indapamide
Active Ingredient(s): 2.5    mg/1 & nbsp;   Indapamide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Indapamide

Product NDC: 0228-2571
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074722
Marketing Category: ANDA
Start Marketing Date: 20070102

Package Information of Indapamide

Package NDC: 0228-2571-96
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0228-2571-96)

NDC Information of Indapamide

NDC Code 0228-2571-96
Proprietary Name Indapamide
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0228-2571-96)
Product NDC 0228-2571
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Indapamide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070102
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name INDAPAMIDE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide-like Diuretic [EPC]

Complete Information of Indapamide


General Information